Fluorinated Ionomer Produced by Aqueous Polymerization Using Dispersed Particulate of Fluorinated Ionomer

ABSTRACT

A process for making an aqueous dispersion of fluorinated ionomer particles by providing dispersed particulate of fluorinated ionomer in an aqueous polymerization medium and polymerizing at least one fluorinated monomer having an ionic group in the aqueous polymerization medium in the presence of the dispersed particulate of fluorinated ionomer and initiator to form the aqueous dispersion of particles of fluorinated ionomer.

FIELD OF THE INVENTION

This invention relates to a process for the dispersion polymerization offluorinated monomer having an ionic group in an aqueous polymerizationmedium and fluorinated ionomer particles and aqueous dispersions madethereby.

BACKGROUND OF THE INVENTION

Fluorinated ionomers are used commercially in the manufacture of ionexchange membranes for electrochemical applications. One industrialapplication is the chloralkali process for the electrolysis of sodiumchloride to produce sodium hydroxide and chlorine. Polymer electrolytemembrane (PEM) fuel cells typically employ fluorinated ionomermembranes. Fluorinated ionomer is also useful as a solid acid catalystfor various chemical processes.

Most known processes for the polymerization of fluorinated ionomercopolymerize tetrafluoroethylene with a fluorinated vinyl ether monomerhaving sulfonyl fluoride group such as is disclosed in U.S. Pat. No.3,282,875, U.S. Pat. No. 4,940,525 and U.S. Pat. No. 7,071,271. Theprocess of U.S. Pat. No. 3,282,875 teaches that it is preferred to carryout polymerization in a perfluorocarbon solvent. U.S. Pat. No. 4,940,525teaches an aqueous polymerization process using the ammonium salt ofperfluorooctanoic acid as a fluorosurfactant. U.S. Pat. No. 7,071,271teaches a process which employs the step of making a pre-emulsion of theSO₂F-comonomer using a microfluidizer prior to the start of thepolymerization process. The pre-emulsion, however, is not stable overtime, i.e., has a “pot life” of at least 1 hour.

Moreover, the copolymerization of tetrafluoroethylene with a fluorinatedvinyl ether monomer with a sulfonyl fluoride group does not produce anionomer directly and instead produce a fluorinated ionomer precursor.Although the sulfonyl fluoride precursor is useful for fabrication ofarticles such as membranes by melt processing, the fluorinated ionomerprecursor must be subjected to a subsequent process step to hydrolyzethe sulfonyl fluoride groups of the polymer sulfonate groups to form theionomer. When ionomer is desired in sulfonic acid form, the ionomer mustbe further treated to convert it to acid form.

A process is desired for the manufacture of fluorinated ionomer whichdirectly produces fluorinated ionomer, especially as a dispersion offluorinated ionomer particles in an aqueous medium.

SUMMARY OF THE INVENTION

The invention is based on the discovery that a process for making anaqueous dispersion of fluorinated ionomer particles is effectivelycarried out by providing dispersed particulate of fluorinated ionomer inan aqueous polymerization medium and polymerizing at least onefluorinated monomer having an ionic group in the aqueous polymerizationmedium in the presence of the dispersed particulate of fluorinatedionomer and initiator to form the aqueous dispersion of particles offluorinated ionomer.

In one preferred form of the present invention, the amount of thedispersed particulate of fluorinated ionomer provided in said aqueouspolymerization medium comprises less than about 15 wt % of saidfluorinated ionomer solids produced in said aqueous dispersion. Inanother preferred form of the invention, the dispersed particulate offluorinated ionomer has a weight average particle size of about 2 nm toabout 100 nm. The fluorinated ionomer preferably has an ion exchangeratio of about 3 to about 53. In a preferred embodiment of theinvention, the fluorinated ionomer is highly fluorinated, morepreferably, perfluorinated.

In a preferred form of the invention, the process further comprisesproviding surfactant in said polymerization medium. Preferably, thesurfactant comprises fluorosurfactant, more preferably, fluoroethersurfactant.

DETAILED DESCRIPTION OF THE INVENTION Fluorinated Ionomer Particulate

Particulate of fluorinated ionomer is employed in the process inaccordance with the present invention. “Fluorinated Ionomer” means afluoropolymer having sufficient ionic groups to provide an ion exchangeratio of no greater than about 53. In this application, “ion exchangeratio” or “IXR” is defined as number of carbon atoms in the polymerbackbone in relation to the ionic groups. Precursor groups such as —SO₂Fwhich upon hydrolysis become ionic are not treated as ionic groups forthe purposes of determining IXR. The fluorinated ionomer employed in theprocess of the invention preferably has an ion exchange ratio of about 3to about 53. More preferably, the IXR is about 3 to about 43, even morepreferably about 3 to about 33, still more preferably about 8 to about33, most preferably 8 to about 23. In a preferred embodiment, thefluorinated ionomer is highly fluorinated. “Highly fluorinated” inreference to ionomer means that at least 90% of the total number ofunivalent atoms bonded to carbon atoms in the polymer are fluorineatoms. Most preferably, the ionomer is perfluorinated.

In fluorinated ionomers, the ionic groups are typically distributedalong the polymer backbone. Preferably, the fluorinated ionomercomprises a polymer backbone with recurring side chains attached to thebackbone with the side chains carrying the ionic groups. Preferredfluorinated ionomer comprises ionic groups having a pKa less than about10, more preferably, less than about 7. Ionic groups of the polymer arepreferably selected from the group consisting of sulfonate, carboxylate,phosphonate, phosphate, and mixtures thereof. The terms “sulfonate,carboxylate, phosphonate and phosphate” are intended to refer to eitherthe respective salts or respective acids from which salts can be formed.Preferably, when salts are employed, the salts are alkali metal orammonium salts. Preferred ionic groups are sulfonate groups. Sulfonategroups in preferred fluorinated ionomers used in the process of theinvention have a pKa of about 1.9 as measured on the fluorinated ionomerin aqueous dispersion form having 10 wt % solids at room temperature.

Various known fluorinated ionomers can be used including polymers andcopolymers of trifluoroethylene, tetrafluoroethylene (TFE),α,β,β-trifluorostyrene, etc., into which ionic groups have beenintroduced. α,β,β-trifluorostyrene polymers useful for the practice ofthe invention are disclosed in U.S. Pat. No. 5,422,411. Possiblepolymers include homopolymers or copolymers of two or more monomers.Copolymers are typically formed from one monomer which is anonfunctional monomer and which provides carbon atoms for the polymerbackbone. A second monomer provides both carbon atoms for the polymerbackbone and also contributes the side chain carrying the ionic group orits precursor, e.g., a sulfonyl fluoride group (—SO₂F), which can besubsequently hydrolyzed to a sulfonate functional group. For example,copolymers of a first fluorinated vinyl monomer together with a secondfluorinated vinyl monomer having a sulfonyl fluoride group (—SO₂F) canbe used. Possible first monomers include tetrafluoroethylene (TFE),hexafluoropropylene, vinyl fluoride, vinylidine fluoride,trifluoroethylene, chlorotrifluoroethylene, perfluoro (alkyl vinylether), and mixtures thereof. Possible second monomers include a varietyof fluorinated vinyl ethers with ionic groups or precursor groups whichcan provide the desired side chain in the polymer. The first monomer mayalso have a side chain. Additional monomers can also be incorporatedinto these polymers if desired.

A class of preferred ionomers for use in the present invention includesa highly fluorinated, most preferably perfluorinated, carbon backboneand the side chain is represented by the formula

—(O—CF₂CFR_(f))_(a)—(O—CF₂)_(b)—(CFR′_(f))_(c)SO₃X,

wherein R_(f) and R^(′) _(f) are independently selected from F, Cl or aperfluorinated alkyl group having 1 to 10 carbon atoms, a=0 to 2, b=0 to1, c=0 to 6, and X is H, Li, Na, K or NH₄. The preferred ionomersinclude, for example, polymers disclosed in U.S. Pat. No. 3,282,875 andin U.S. Pat. Nos. 4,358,545 and 4,940,525. One preferred ionomercomprises a perfluorocarbon backbone and the side chain is representedby the formula —O—CF₂CF(CF₃)—O—CF₂CF₂SO₃X, wherein X is as definedabove. Ionomers of this type are disclosed in U.S. Pat. No. 3,282,875and can be made by copolymerization of tetrafluoroethylene (TFE) and theperfluorinated vinyl ether CF₂═CF—O—CF₂CF(CF₃)—O—CF₂CF₂SO₂F,perfluoro(3,6-dioxa-4-methyl-7-octenesulfonyl fluoride) (PDMOF),followed by conversion to sulfonate groups by hydrolysis of the sulfonylfluoride groups and ion exchanging if needed to convert to the desiredform. One preferred ionomer of the type disclosed in U.S. Pat. Nos.4,358,545 and 4,940,525 has the side chain —O—CF₂CF₂SO₃X, wherein X isas defined above. This ionomer can be made by copolymerization oftetrafluoroethylene (TFE) and the perfluorinated vinyl etherCF₂═CF—O—CF₂CF₂SO₂F, perfluoro(3-oxa-4-pentenesulfonyl fluoride) (POPF),followed by hydrolysis and acid exchange if needed.

For ionomers of this type, the cation exchange capacity of a polymer isoften expressed in terms of equivalent weight (EW). For the purposes ofthis application, equivalent weight (EW) is defined to be the weight ofthe ionomer in acid form required to neutralize one equivalent of NaOH.In the case of a sulfonate ionomer where the ionomer comprises aperfluorocarbon backbone and the side chain is—O—CF₂—CF(CF₃)—O—CF₂—CF₂—SO₃H (or a salt thereof), the equivalent weightrange which corresponds to an IXR of about 8 to about 23 is about 750 EWto about 1500 EW. IXR for this ionomer can be related to equivalentweight using the following formula: 50 IXR+344=EW. While generally thesame IXR range is used for sulfonate ionomers disclosed in U.S. Pat.Nos. 4,358,545 and 4,940,525, e.g., the ionomer having the side chain—O—CF₂CF₂SO₃H (or a salt thereof), the equivalent weight is somewhatlower because of the lower molecular weight of the monomer unitcontaining the ionic group. For the preferred IXR range of about 8 toabout 23, the corresponding equivalent weight range is about 575 EW toabout 1325 EW. IXR for this polymer can be related to equivalent weightusing the following formula: 50 IXR+178=EW.

The molecular weight of the fluorinated ionomer particulate cangenerally be in the same range as the resin which is used in ionexchange polymer membranes used in the chloralkali process for theelectrolytic production of chlorine and sodium hydroxide from sodiumchloride and in fuel cells. Such fluorinated ionomer resin has amolecular weight which preferably provides solid fluorinated ionomerparticulate at room temperature. In thermoplastic forms of thefluorinated ionomer, melt flow rate is preferably in the range of 1 toabout 500, more preferably about 5 to about 50, most preferably about 10to about 35 g/10 min.

The fluorinated ionomer particulate of the dispersion employed inaccordance with the process of the invention preferably has a weightaverage particle size of about 2 nm to about 100 nm. More preferably,such particulate has a weight average particle size of about 2 to about50 nm, even more preferably about 2 to about 30, still more preferablyabout 2 to about 10 nm. A suitable preparation method for aqueousdispersions of such fluorinated ionomer particulate is taught in U.S.Pat. Nos. 6,552,093 and 7,166,685 (Curtin et al.). The preparationmethod of Curtin et al. can provide “water only” aqueous dispersions.“Water only” means the aqueous dispersions contain a liquid medium whichcontains either no other liquids other than water or, if other liquidsare present, no more that about 1 wt %, of such liquids.

The weight average particle size in a liquid dispersion of fluorinatedionomer particulate used in accordance with the invention can bemeasured by a dynamic light scattering (DLS) technique as describedbelow in the Test Methods.

In accordance with the invention, dispersed fluorinated ionomerparticulate is preferably provided in the aqueous polymerization mediumby mixing a concentrated aqueous dispersion or dispersible powder of thefluorinated ionomer into the aqueous polymerization medium. Preferredconcentrated aqueous dispersions for use in accordance with theinvention are preferably the “water only” aqueous dispersions describedabout made as taught in U.S. Pat. Nos. 6,552,093 and 7,166,685 (Curtinet al.). Solids levels in such concentrates are preferably about 1 toabout 35 wt %, more preferably about 5 to about 35 wt %. Aqueousdispersions made as disclosed in U.S. Pat. Nos. 6,552,093 and 7,166,685B2 (Curtin et al.) can also be dried to form powders which are readilyredispersed in water or various polar organic solvents to providedispersions in such solvents. While dispersions of fluorinated ionomerparticulate in polar organic solvents may be useful in the practice ofthe invention, such solvents are usually telogenic and it is generallypreferred to employ aqueous dispersions of the fluorinated ionomer inthe practice of the present invention with low amounts or no organicsolvents present. Thus, dried powders of the dispersions made accordingto U.S. Pat. Nos. 6,552,093 and 7,166,685 B2 (Curtin et al.) can beintroduced directly into the aqueous polymerization medium or mixed withwater to produce a concentrated aqueous dispersion prior to suchintroduction to provide the dispersion of fluorinated ionomerparticulate. Concentrated aqueous dispersions, whether made directlyfrom the process as disclosed in U.S. Pat. Nos. 6,552,093 and 7,166,685B2 (Curtin et al.) or made from dried powders, can be produced andstored at concentrations up to 35 wt % solids, are stable for longperiods, and can be diluted to any desired concentration with water.

Suitable fluorinated ionomer dispersions may also be available in, forexample, mixed solvents of water and lower alcohols as disclosed in U.S.Pat. No. 4,443,082 (Grot). The alcohol content of such dispersions maybe reduced or substantially removed using, for example, a rotaryevaporator.

Fluorinated Ionomer Particles Produced in the Process

The fluorinated ionomer of the fluorinated ionomer particles produced bythe process of the invention can be of the same type as described abovefor the fluorinated ionomer of the fluorinated ionomer particulateexcept that the fluorinated ionomer is produced directly due to thefluorinated monomer being employed with the ionic group in ionic formduring polymerization, i.e., as the acid or salt. The type of monomersemployed, the types ionic groups, whether in the ionic groups are inacid or salt form, IXR, melt flow, dispersion concentration, weightaverage particle size and other properties are selected based on thedesired end use properties and the selected conditions employed in thepolymerization process of the invention employed as will be described inmore detail hereinafter.

Surfactant

In addition to a dispersion of fluorinated ionomer particulate, theaqueous polymerization medium used to form the aqueous dispersion ofparticles of fluoropolymers may further comprise surfactant. Thesurfactant can be selected from a large group of suitable surfactantsincluding hydrocarbon surfactants, siloxane surfactants, andfluorosurfactants. Suitable hydrocarbon surfactants have been disclosedin U.S. Pat. No. 5,925,705 to Araki et al; and JP Patent Publications2004/358397 and 2004/359870 to Tsuda et al. Suitable siloxanesurfactants have been described in U.S. Pat. No. 6,841,616 to Wille etal. Preferably the surfactant is a fluorosurfactant and more preferablyis a fluoroether surfactant.

Examples of fluorosurfactants that may be a component of thepolymerization agent are described in U.S. Pat. No. 6,395,848 to Morganet al. as fluoroalkyl having at most one ether oxygen, preferablyperfluoroalkyl, carboxylic acids and salts thereof having 6-20 carbonatoms, preferably 6-12 carbon atoms, such as ammonium perfluorooctanoateand ammonium perfluorononanoate (see Berry, U.S. Pat. No. 2,559,752).Perfluoroalkyl sulfonic acids and salt may also be used. In a preferredembodiment of the invention, perfluoroalkyl ethane sulfonic acids andsalts thereof are employed, preferably a compound or a mixture ofcompounds of the formula F—(—CF₂—CF₂—)_(n)—CH₂CH₂—SO₃M, wherein n is 2-8and M is a cation having a valence of 1 as described in Khan & Morgan,U.S. Pat. No. 4,380,618. More preferably, such perfluoroalkyl ethanesulfonic acid surfactant comprises a compound of the formulaC₆F₁₃—CH₂CH₂—SO₃M, wherein M is a cation having a valence of 1 asdescribed in Baker & Zipfel, U.S. Pat. Nos. 5,688,884 and 5,789,508.Preferably, M in the above formula is NH₄ ⁺.

Additional examples of such fluorosurfactants include perfluoroalkoxybenzene sulfonic acids and salts thereof wherein the perfluoroalkylcomponent of the perfluoroalkoxy has 4-12 carbon atoms, preferably 7-12carbon atoms (as described in Morgan, U.S. Pat. No. 4,621,116).Additional examples of such surfactants also includepartially-fluorinated surfactants having internal methylene groups andhaving the formula R_(f)—(CH₂)_(m)—R′_(f)—COOM wherein m is 1-3, R_(f)is perfluoroalkyl or perfluoroalkoxy containing 3-8 carbon atoms, R′_(f)is linear or branched perfluoroalkylene containing 1-4 carbon atoms, andM is NH₄, Li, Na, K, or H (as described in Feiring et al., U.S. Pat. No.5,763,552).

Examples of suitable fluoroether surfactants have been described in U.S.Pat. No. 3,271,341 to Garrison; U.S. Patent Publications 2007/0015864,2007/0015865, and 2007/0015866 to Hintzer et al.; U.S. PatentPublications 2005/0090613 to Maruya et al. and 2006/0281946 to Morita etal.; PCT Patent Publications WO 2007046345 to Higuchi et al., 2007046377to Funaki et al., 2007046482 to Hoshikawa et al., and 2007/049517 toMatsuoka et al.

In accordance with a preferred embodiment of the invention, the aqueousmedium comprises less than about 300 ppm of perfluoroalkane carboxylicacid or salt fluorosurfactants having 8 or more carbon atoms, based onthe weight of water in the aqueous medium. Perfluoroalkane acid or saltfluorosurfactants having 8 or more carbon atoms include such surfactantshaving for example 8-14 carbon atoms, e.g., perfluorooctanoic acid andsalts and perfluorononanoic acid and salts. More preferably, the aqueousmedium comprises less than about 100 ppm of perfluoroalkane carboxylicacid or salt fluorosurfactants having 8 or more carbon atoms, morepreferably less than 50 ppm. In a preferred embodiment of the invention,the aqueous medium is substantially free of perfluoroalkane carboxylicacid or salt fluorosurfactants having 8 or more carbon atoms.Substantially free of perfluoroalkane carboxylic acid or saltfluorosurfactants having 8 or more carbon atoms means that aqueousmedium contains no more than about 10 ppm of such fluorosurfactants.

In a preferred embodiment the aqueous polymerization medium contains ashort chain fluorosurfactant having the formula:

[R¹-O_(n)-L-A⁻]Y⁺  (I)

wherein:

-   -   R¹ is a linear or branched partially or fully fluorinated        aliphatic group which may contain ether linkages;

n is 0 or 1;

L is a linear or branched alkylene group which may be nonfluorinated,partially fluorinated or fully fluorinated and which may contain etherlinkages;

A⁻ is an anionic group selected from the group consisting ofcarboxylate, sulfonate, sulfonamide anion, and phosphonate; and

Y⁺ is hydrogen, ammonium or alkali metal cation; with the proviso thatthe chain length of R¹-O_(n)-L- is not greater than 6 atoms.

“Chain length” as used in this application refers to the number of atomsin the longest linear chain in the hydrophobic tail of thefluorosurfactant employed in the process of this invention. Chain lengthincludes atoms such as oxygen atoms in addition to carbon in the chainof the hydrophobic tail of the surfactant but does not include branchesoff of the longest linear chain or include atoms of the anionic group,e.g., does not include the carbon in carboxylate. “Short chain” as usedin this application refers to a chain length of not greater than 6.“Long chain” refers to a chain length of greater than 6, e.g.,fluorosurfactants having a chain length of 7 to 14 atoms.

Preferably, the chain length of R¹-O_(n)-L- is 3 to 6 atoms. Inaccordance with one preferred form of the invention the chain length ofR¹-O_(n)-L- is 4 to 6 atoms. In accordance with another preferred formof the invention the chain length of R¹-O_(n)-L- is 3 to 5 atoms. Mostpreferably, the chain length of R¹-O_(n)-L- is 4 to 5 atoms. A preferredclass of fluorosurfactants is short chain fluoroether acids or salts,i.e., wherein n is 1 in Formula (I) above. Preferred fluoroether acidsor salts in accordance with the invention are fluorosurfactantsaccording to Formula (I) wherein:

R¹ is a linear or branched partially or fully fluorinated alkyl grouphaving 1 to 3 carbon atoms which may contain ether linkages; and

L is an alkylene group selected from —CX(R²)—, wherein R² is fluorine orperfluoromethyl and X is hydrogen or fluorine, and —CZ¹Z²CZ³Z⁴—, whereinZ¹, Z², Z³, and Z⁴ are independently selected from hydrogen or fluorine.

Fluoroether acids and salts of this type are known. When L is analkylene group selected from —CX(R²)—, wherein R² is fluorine orperfluoromethyl and X is hydrogen or fluorine, the compound can be made,for example, by hydrolysis of perfluoro-2-alkoxypropionyl fluorideintermediates prepared by reacting alkanoic acid fluorides withhexafluoropropylene oxide as disclosed in U.S. Pat. No. 3,291,843 toFritz and Selman for use in perfluoro(alkyl vinyl ether) manufacture.When L is —CZ₂CZ₂—, wherein Z is independently selected from hydrogen orfluorine, routes to making such compounds are generally described InU.S. Pat. No. 2,713,593 (Brice et al.) where fluoro(alkoxypropionic)acids and derivatives are obtained in useful yields from correspondinghydrocarbon alkoxypropionic acids and derivatives by electrochemicalfluorination. Fully fluorinated and partially fluorinated products canbe separated for example by fractional distillation. Useful teachingsfor synthesis can also be found in EP 0 148 482 B1 (Ohsaka et al.) forpartially fluorinated propoxy propionic acid fluoride which may befurther fluorinated or perfluorinated by electrofluorinating the acidfluoride which is then easily converted to an acid or salt.

In accordance with another preferred form of the invention, L in Formula(I) is an alkylene group selected from —CF(CF₃)—, —CF₂—, —CF₂CF₂—,—CHFCF₂—, and —CF₂CHF—.

The fluorosurfactant used in accordance with the invention may be adiether if R1 or L contains ether linkages. Such compounds are made, forexample, by the teachings in WO 01/46116 A1 (Hintzer et al.). Preferredfluoroether acids or salts are fluoromonoethers where R¹ and L do notcontain ether linkages.

In accordance with another preferred form of the invention, R¹ inFormula (I) is a linear partially or fully fluorinated alkyl grouphaving 2 to 3 carbon atoms. Preferably, R¹ is fully fluorinated.

In accordance with another preferred form of the invention, thefluorosurfactant is highly fluorinated. “Highly fluorinated” inreference to fluorosurfactant means that at least about 50% of the totalnumber of univalent atoms bonded to carbon in the fluorosurfactant arefluorine atoms. More preferably, at least about 75% of the total numberof univalent atoms bonded to carbon in the fluorosurfactant are fluorineatoms, most preferably at least about 90%. Perfluorinated surfactantsare also preferred for use in accordance with the invention.

In accordance with one preferred embodiment of the invention, thefluorosurfactant is a compound of the formula:

[CF₃CF₂CF₂OCF(CF₃)COO⁻]Y⁺  (II)

wherein Y⁺ is hydrogen, ammonium, or alkali metal cation. This compoundis represented by Formula (I) wherein R¹ is CF₃CF₂CF₂—; L is —CF(CF₃)—;A⁻ is carboxylate; and Y⁺ is hydrogen, ammonium or alkali metal cation.Preferably, Y⁺ is hydrogen or ammonium. A compound of this formula canbe obtained from the perfluoro-2-propoxypropionyl fluoride intermediateprepared according to U.S. Pat. No. 3,291,843 or by dimerization ofhexafluoropropylene oxide and subsequent hydrolysis of the resultingacid fluoride to carboxylic acid in the case of the acid and, in thecase of the salt, by simultaneous or subsequent reaction with theappropriate base to produce the desired salt. A procedure fordimerization of hexafluoropropylene oxide is disclosed in G.B. Patent1,292,268.

In accordance with another preferred embodiment of the invention, thefluorosurfactant is a compound of the formula:

[CF₃CF₂OCF(CF₃)COO⁻]Y⁺  (III)

wherein Y⁺ is hydrogen, ammonium, or alkali metal cation. A compound ofthis formula can be obtained from the perfluoro-2-ethoxypropionylfluoride intermediate prepared according to U.S. Pat. No. 3,291,843 andsubsequent hydrolysis of the resulting acid fluoride to carboxylic acidin the case of the acid and, in the case of the salt, by simultaneous orsubsequent reaction with the appropriate base to produce the desiredsalt.

In accordance with other embodiments of the invention, thefluorosurfactant is a compound of the formula:

[C₂F₅OCF₂CF₂CF₂COO⁻]Y⁺  (IV)

[C₃F₇OCF₂COO⁻]Y⁺  (V)

[C₃F₇OCF₂CF₂COO⁻]Y⁺  (VI)

[C₃F₇OCF₂CF₂CF₂COO⁻]Y⁺  (VII)

wherein Y⁺ is hydrogen, ammonium, or alkali metal cation. Thesecompounds can be made, for example, by the procedures described in U.S.Patent Publication 2007/0015864 (Hintzer et al.).

In accordance with another embodiment of the invention, thefluorosurfactant is a compound of Formula (I) wherein n is 0; R¹ and Lcollectively comprises a perfluoroalkyl group having 4-6 carbons; and A⁻is sulfonate and sulfonamide anion. In a preferred embodiment of thisform of the invention, A⁻ is sulfonamide anion, the sulfonamide compoundof Formula (VIII) below:

[C₄F₉SO₂N⁻CH₂CH₂OH]Y⁺  (VIII)

wherein Y⁺ is hydrogen, ammonium, or alkali metal cation. A surfactantof this formula as the ammonium salt is available commercially from 3Munder the trademark NOVEC™ 4200.

In accordance with another embodiment of the invention, thefluorosurfactant is a compound of the formula:

[CF₃CF₂CF₂CF₂CH₂CH₂SO₃ ⁻]Y⁺  (IX)

wherein Y⁺ is hydrogen, ammonium, or alkali metal cation.

The surfactant can be added to the aqueous polymerization medium priorto, simultaneously with and/or subsequently to the addition of thedispersion of fluorinated ionomer particulate. In a preferredembodiment, the surfactant is supplied in salt form. If the surfactantis supplied as the corresponding acid, conversion to salt can beaccomplished by adding ammonium hydroxide or alkali metal hydroxide,preferably ammonium hydroxide, to a solution of the acid in a quantitysufficient to substantially completely convert the acid to salt formprior to adding the surfactant to the aqueous polymerization medium.Alternatively the surfactant supplied in acid form can be added to theaqueous polymerization medium and subsequently converted to salt form.

Initiators

Polymerization in accordance with the invention employs free radicalinitiators capable of generating radicals under the conditions ofpolymerization. As is well known in the art, initiators for use inaccordance with the invention are selected based on the type offluoropolymer and the desired properties to be obtained, e.g., end grouptype, molecular weight, etc. Water-soluble salts of inorganic peracidsare suitably employed which produce anionic end groups in the polymer.Preferred initiators of this type have a relatively long half-life atthe temperature of polymerization, preferably persulfate salts, e.g.,ammonium persulfate or potassium persulfate. To shorten the half-life ofpersulfate initiators, reducing agents such as ammonium bisulfite orsodium metabisulfite, with or without metal catalyst salts such as iron,can be used. Preferred persulfate initiators are substantially free ofmetal ions and most preferably are ammonium salts.

The initiator is added to the aqueous polymerization medium in an amountsufficient to initiate and maintain the polymerization reaction at adesired reaction rate. At least a portion of the initiator is preferablyadded at the beginning of the polymerization. A variety of modes ofaddition may be used including continuously throughout thepolymerization, or in doses or intervals at predetermined times duringthe polymerization. A particularly preferred mode of operation is forinitiator to be precharged to the reactor and additional initiator to becontinuously fed into the reactor as the polymerization proceeds.Preferably, total amounts of ammonium persulfate and/or potassiumpersulfate employed during the course of polymerization are about 25 ppmto about 250 ppm based on the weight of the aqueous medium. Other typesof initiators, for example, potassium permanganate/oxalic acidinitiators, can be employed in amounts and in accordance with proceduresas known in the art.

Chain Transfer Agents

Chain-transfer agents may be used in a process in accordance with theinvention to decrease molecular weight for the purposes of controllingmelt viscosity. Chain transfer agents useful for this purpose arewell-known for use in the polymerization of fluorinated monomers.Preferred chain transfer agents include hydrogen, aliphatichydrocarbons, halocarbons, hydrohalocarbons or alcohol having 1 to 20carbon atoms, more preferably 1 to 8 carbon atoms. Representativepreferred examples of such chain transfer agents are alkanes such asethane, chloroform, 1,4-diiodoperfluorobutane and methanol.

The amount of a chain transfer agent and the mode of addition depend onthe activity of the particular chain transfer agent and on the desiredmolecular weight of the polymer product. A variety of modes of additionmay be used including a single addition before the start ofpolymerization, continuously throughout the polymerization, or in dosesor intervals at predetermined times during the polymerization. Theamount of chain train transfer agent supplied to the polymerizationreactor is preferably about 0.005 to about 5 wt %, more preferably fromabout 0.01 to about 2 wt % based upon the weight of the resultingfluorinated ionomer.

Process

In the practice of a preferred embodiment of the invention, the processis carried out as a batch process in a pressured reactor. Suitablevertical or horizontal reactors for carrying out the process of theinvention are equipped with stirrers for the aqueous medium to providesufficient contact of gas phase monomers such as TFE for desirablereaction rates and uniform incorporation of comonomers if employed. Thereactor preferably includes a cooling jacket surrounding the reactor sothat the reaction temperature may be conveniently controlled bycirculation of a controlled temperature heat exchange medium.

In a typical process, the reactor is first charged with deionized anddeaerated water of the polymerization medium and the fluorinated ionomerparticulate is dispersed in the medium. If used, surfactant is suitableprecharged and/or fed to the reactor as the reaction proceeds. Asuitable procedure for a copolymer of TFE andperfluoro(3,6-dioxa-4-methyl-7-octenesulfonate (PDMOS) monomer (eitheracid or salt form) includes first pressurizing the reactor with TFE. Thecomonomer PDMOS is then added. A free-radical initiator solution such asammonium persulfate solution is then added. The temperature is increasedand, once polymerization begins, additional TFE is added to maintain thepressure. The beginning of polymerization is referred to as kick-off andis defined as the point at which gaseous monomer feed pressure isobserved to drop substantially, for example, about 5-10 psi (about 35-70kPa). Comonomer and/or chain transfer agent can also be added as thepolymerization proceeds. For some polymerizations, surfactant and/orinitiator may be added during the polymerization.

Batch dispersion polymerizations can be described as proceeding in twophases. The initial period of the reaction can be said to be anucleation phase during which a given number of particles areestablished. Subsequently, it can be said that a growth phase occurs inwhich the predominant action is polymerization of monomer on establishedparticles with little or no formation of new particles. The transitionfrom the nucleation to the growth phase of polymerization occurssmoothly, typically between about 4 and about 10 percent solids in thepolymerization.

The use of fluorinated ionomer in accordance with the inventiongenerally provides sufficient nucleation for the polymerization processand additional nucleating agents are not required. It is not necessaryfor stabilizing surfactants, if used, to provide additional nucleationalthough surfactants capable of effective nucleation may be used ifdesired. In accordance with one embodiment of the present invention, thenumber of dispersed fluorinated ionomer particles in the particulateintroduced into the polymerization medium is preferably selected tocontrol the number of particles formed during the nucleation phase.Preferably, the fluorinated ionomer particulate in the aqueouspolymerization medium provides a number of dispersed fluorinated ionomerparticles within about 15% of the number of fluoropolymer particlesproduced by polymerizing the fluorinated monomer. More preferably, thenumber of dispersed fluorinated ionomer particles is within about 10% ofthe number of fluoropolymer particles produced by polymerizing, morepreferably, the number of dispersed fluorinated ionomer particles iswithin about 5% of the number of fluoropolymer particles produced bypolymerizing. Most preferably, the number of dispersed fluorinatedionomer particles is approximately equal to the number of fluoropolymerparticles produced by polymerizing. The amount of fluoropolymerparticulate to be employed in a process in accordance with the inventionmay be determined by estimating the number of fluoropolymer particles tobe produced in the process based on particle size and solids content andemploying an amount of fluorinated ionomer particulate which providesapproximately the same number of particles. If other nucleating agentsare also employed in the polymerization, it may be desirable to employ asmaller number of particles of fluorinated ionomer particulate. Typicalconcentrations of dispersed fluorinated ionomer particulate are about1×10¹⁶ particles per liter to about 1×10²⁰ particles per liter.

Preferably, the amount of fluorinated ionomer particulate provided inthe aqueous polymerization medium comprises less than about 15 weight %of the fluoropolymer solids to be produced in the process. In morepreferred embodiments the amount of fluorinated ionomer particulateprovided in the aqueous polymerization medium comprises less than about10 wt %, and even more preferably less than about 1 wt %, still morepreferably about 0.1 wt % of the fluoropolymer solids to be produced inthe process and most preferably less than 0.025 wt % of thefluoropolymer solids.

If used, the amount of surfactant employed is dependent upon the desiredsolids content for the polymerization, the type of surfactant, the typeof fluoropolymer being produced, reactor design, etc. The amountsemployed can be similar to the amounts employed in conventionalpolymerizations which do not employ fluorinated ionomer particulate.

Typical amounts are about 0.01 wt % to about 1 wt % based on the weightof water in the polymerization medium. When a surfactant is used whichis capable of effective nucleation, the amount employed typically willbe less than the amount employed in a conventional polymerizationwithout the use of fluorinated ionomer particulate.

The solids content of the dispersion upon completion of polymerizationcan be varied depending upon the intended use for the dispersion. Thesolids content of fluoropolymer dispersion produced by the process ofthe invention is preferably at least about 10 wt %. More preferably, thefluoropolymer solids content is at least about 20 wt %. A preferredrange for fluoropolymer solids content produced by the process is about20 wt % to about 65 wt %, even more preferably about 20 wt % to about 55wt %, most preferably, about 35 wt % to about 55 wt %.

After batch completion (typically several hours) when the desired amountof polymer or solids content has been achieved, the feeds are stopped,the reactor is vented and purged with nitrogen, and the raw dispersionin the vessel is transferred to a cooling vessel. In a preferred processof the invention, polymerizing produces less than about 13 wt %, morepreferably less than about 10 wt %, still more preferably less than 3 wt%, even more preferably less than 1 wt %, most preferably less thatabout 0.5 wt % of undispersed fluoropolymer (coagulum) based on thetotal weight of fluoropolymer produced.

In one embodiment of the invention, the aqueous dispersion offluoropolymer particles has a raw dispersion particle size (RDPS) offrom about 10 to about 400 nm, preferably 100 to 350 nm.

The aqueous dispersions of fluorinated ionomer particles produced inaccordance with the invention typically are stable as produced but canbe further stabilized with anionic, cationic, or nonionic surfactant forcertain uses. The fluorinated ionomer can also be isolated from thedispersion by coagulation and removal of the aqueous medium. Sulfonatepolymers in acid form can be melt-processed for some applications. Forthis use, the fluorinated ionomer is dried then processed into aconvenient form such as flake, chip or pellet for use in subsequentmelt-processing operations.

The process of the invention may also be carried out as a continuousprocess in a pressurized reactor.

Polymerization Products

The process of the invention directly produces fluorinated ionomer and ahydrolysis step is not required as in prior art processes. Thefluorinated ionomer may be produced in acid or salt form as may bedesired for end use applications. Preferably, the fluorinated ionomer ofthe particulate has an ion exchange ratio of about 3 to about 53.Preferably, the fluorinated ionomer is highly fluorinated, mostpreferably perfluorinated.

In a preferred embodiment of the invention, the fluorinated ionomercomprises a polymer backbone with recurring side chains attached to thepolymer backbone with the side chains carrying ionic groups. Ionicgroups are preferably selected from the group consisting of sulfonate,carboxylate, phosphonate, phosphate and mixtures thereof. Preferably,the fluorinated ionomer of the particulate comprises ionic groups havinga pKa less than about 10. Sulfonate groups are most preferred.

In a preferred embodiment of the invention, the fluorinated ionomer hasrecurring side chains represented by the formula—(O—CF₂CFR_(f))_(a)—(O—CF₂)_(b)—(CFR′_(f))_(c)SO₃X, wherein R_(f) andR′_(f) are independently selected from F, Cl or a perfluorinated alkylgroup having 1 to 10 carbon atoms, a=0 to 2, b=0 to 1, c=0 to 6, and Xis H, Li, Na, K or NH₄. More preferably, the recurring side chain isrepresented by the formula —O—CF₂CF(CF₃)—O—CF₂CF₂—SO₃X wherein X is H,Li, Na, K or NH₄. Preferably, fluorinated ionomer produced by theprocess has a melt flow in thermoplastic form at 270° C. using a 5 kgweight of about 1 to about 500.

The fluorinated ionomer particles made using the process of theinvention can be employed generally in the same manner as fluorinatedionomer made conventionally except that hydrolysis is not required toconvert the as-polymerized polymer to ionomer. Aqueous dispersions ofthe fluorinated ionomer particles can be used for to produce coatings ona variety of substrates and cast to make films useful as ion exchangemembranes useful in electrochemical processes and devices, for example,as membranes in the chloralkali process and in fuel cells. Meltprocessable fluorinated ionomer coagulated from the dispersion can bemelt extruded into films for similar uses in the chloralkali process andin fuel cells. The aqueous dispersions of fluorinated ionomer particles,as well as coating and articles produced, are also useful for acidcatalyst applications.

Test Methods

Melt Flow Rate (MFR) of the Fluorinated Ionomer is measured on thepolymer in thermoplastic form, e.g., the sulfonyl fluoride or sulfonicacid form for sulfonate ionomers, according to the method of ASTMD-1238-04c at 270° C. with a 2110 gram weight.

Fluorinated Ionomer Particulate Size, Weight Average, is measured bydynamic light scattering (DLS). Dispersions of the ionomers were dilutedfrom 10× to 100× (vol:vol), but typically 30×, into a dispersant ofdimethyl sulfoxide with additives of 0.1 wt % (solids basis) of Zonyl®1033D (C₆F₁₃CH₂CH₂SO₃H) surfactant and 0.23 wt % ethyldiisopropylamine,which neutralized the Zonyl® and the ionomer end groups totrialklyammonium forms. This dispersant mixture was called “DMSOZE”. Thediluted dispersion was filtered through a 1.0 um graded density glassmicro fiber syringe filter (Whatman PURADISC® #6783-2510) into adisposable polystyrene cuvette. Dynamic light scattering (DLS) wasmeasured at 25° C. using a Malvern Instruments Nano S, which measuresscattered light from a HeNe laser at 633 nm at a scattered angle of 173°(close to backscattered). The automated instrument chooses how many 10 sruns make up each measurement (generally 12 to 16), and for each sampleten measurements were performed, the entire process taking usually ˜30min. For concentrated or highly scattering samples, the instrument maymove the focal point of the laser close to the front of the cuvette,minimizing the path length through the sample and thus reducingparticle-particle scattering artifacts. However, for almost all thefluorinated ionomer dispersion samples analyzed here, the instrumentchose to use a focal position of 4.65 mm, which maximized the path inthe cell and enhanced detection of the weak scattering. In addition, theinstrument adjusts an attenuator to maintain the count rate in anoptimum range. The attenuator settings were 11, 10, or 9, whichcorrespond to light attenuation factors of ×1.00 (no attenuation),×0.291, or ×0.115, respectively. Various numeric and graphical outputsare available from the Malvern software. The simplest and most robust isthe “z-average” particle diameter, calculated from the z-averagediffusion coefficient made by a cumulants fit to the autocorrelationfunction. The name z-average has been used in analogy to the z-averagemolecular weight M_(i) ², in that the DLS z-average particle size isderived from a distribution of diffusion coefficients weighted by thesquare of the particle mass M_(i) ². Half of the scattered lightIntensity is produced by particles with diameters larger than D(I)50.Using the input refractive index of the particles, dispersant index,wavelength, and scattering angle, the software uses a Mie calculation toconvert the intensity distribution to a weight distribution. The weightaverage diameter is that diameter at which half of the mass of theparticles in the sample have a larger diameter and half have a smallerdiameter.

Dry coaqulum amount is measured by physically collecting the wet polymerthat coagulates during the course of the polymerization and then dryingthis coagulum overnight at 80° C. and a vacuum of 30 mm Hg (4 kPa). Thedried coagulum is weighed and the Weight Percentage of UndispersedPolymer (Coaq. wt %) is determined based on the total weight offluoropolymer in the dispersion.

Transition Temperatures of Fluoropolymers by Differential ScanningCalorimetry (DSC) is measured according to ASTM D 3418-03.

Comonomer Content is measured by FTIR according to the method disclosedin U.S. Pat. No. 4,743,658, col. 5, lines 9-23.

Fluorinated Ionomer Particle Size, i.e., raw dispersion particle size(RDPS) of the fluorinated ionomer produced in the process is determinedby laser diffraction techniques that measure the particle sizedistributions (PSD) of materials using a Microtrac Ultrafine ParticleAnalyzer (UPA). The UPA uses dynamic light scattering principle formeasuring PSD with size range of 0.003 micron to 6.54 micron. Thesamples were analyzed after collecting the background with water. Themeasurements were repeated three times and averaged.

Perfluoroalkane Carboxylic Acid or Salt Fluorosurfactant Content ismeasured by a GC technique in which the fluorosurfactant is esterifiedwith acidic methanol. Perfluoroheptanoic acid is used as an internalstandard. Upon addition of electrolyte and hexane the ester is extractedinto the upper hexane layer. The hexane layer is analyzed by injectiononto a glass GC column of 20 ft.×2 mm I.D. packed with 10% OV-210 on70/80 mech Chromosorb W.AW.DMCS. held at 120 C. The detector is ECD andthe carrier gas of 95% argon/5% methane has a flow rate of 20 to 30ml/min.

EXAMPLE Fluorinated Ionomer Particulate

Aqueous dispersion of fluorinated ionomer particulate (FI) is preparedaccording to the procedure described as Example 4 in U.S. Pat. No.7,166,685, (fluorinated ionomer in the acid form) using TFE/PDMOFfluorinated ionomer resin having an IXR of 12.1 (EW of 950) and a meltflow in its sulfonyl fluoride form of 24. The aqueous dispersion offluorinated ionomer particulate has a solids content of 21.4 wt % withthe fluorinated ionomer particulate having a weight average diameter of5.23 nm. The ionic groups have a pKa of about 1.9 as measured on thefluorinated ionomer in aqueous dispersion form having 10 wt % solids atroom temperature.

Surfactant

For use in Example 1 below, the surfactant: C₃F₇OCF(CF₃)COONH₄ (HFPOdimer acid salt, DAS), 20 wt %, is prepared by dropwise addition of 128g of concentrated ammonium hydroxide solution to 500 g ofC₃F₇OCF(CF₃)COOH and subsequent dilution with deionized water to 20 wt%.

Example 1 TFE/PDMOS Polymerization Using Dispersed Fluorinated IonomerParticulate

This example demonstrates the polymerization of TFE/PDMOS fluorinatedionomer copolymer in the presence of dispersed particulate offluorinated ionomer in a 1 gallon (3.8 liter) reactor.

A cylindrical, horizontal, water-jacketed, paddle-stirred, stainlesssteel reactor having a length to diameter ratio of about 1.5 and a watercapacity of 1 gallon (3.8 liter) is charged with 1750 grams ofdemineralized water, 1.4 g of a dispersion of 20 wt % aqueous solutionof fluorinated ionomer particulate, and 20 grams of a 20 wt % aqueoussolution of DAS. With the reactor paddle agitated at 110 rpm, thereactor is heated to 25° C. and then evacuated and purged three timeswith tetrafluoroethylene (TFE). The reactor temperature is increased to65° C., and is pressured to 30 psig (0.31 MPa) with TFE. Then 40 ml offreshly prepared aqueous initiator solution containing 0.5% ammoniumpersulfate (APS) is injected. Then, this same initiator solution ispumped into the reactor at 0.1 ml/min. After polymerization has begun asindicated by a 5 psi (35 KPa) drop in reactor pressure (kickoff),additional TFE is fed into the reactor at a rate of 0.5 gram/minute.After 5 grams of TFE have been consumed after kickoff, 100 ml ofperfluoro(3,6-dioxa-4-methyl-7-octene)sulfonic acid is injected followedby 0.25 ml/min of perfluoro(3,6-dioxa-4-methyl-7-octene)sulfonic acidfor the remainder of the batch. At the same time, 0.25 ml/min of thesame 0.2 wt % APS solution is injected for the remainder of the batch.The TFE feed rate is adjusted to 1.13 g/minute. After 60 minutes (67.8additional grams of TFE consumed), the reaction is terminated. At theend of the reaction period, the feeds are stopped, and the reactor isslowly vented. After venting to nearly atmospheric pressure, the reactoris purged with nitrogen to remove residual monomer. Upon furthercooling, the dispersion is discharged from the reactor at below 35° C.The solids content of the raw dispersion is 7.1 wt % and the rawdispersion particle size (RDPS) is 74 nm.

The dispersion is coagulated by freezing and thawing. After coagulation,the polymer is isolated by filtering and then drying in a 150° C.convection air oven. The isolated polymer contains 48 wt %perfluoro(3,6-dioxa-4-methyl-7-octene)sulfonic acid (IXR=13.6, EW=1025)and has a melt flow rate measured by ASTM D-1238-04c at 270° C. with a2110 gram weight of 23.4 grams/10 minutes.

1. A process for making an aqueous dispersion of fluorinated ionomerparticles comprising: providing dispersed particulate of fluorinatedionomer in an aqueous polymerization medium; polymerizing at least onefluorinated monomer having an ionic group in said aqueous polymerizationmedium in the presence of said dispersed particulate of fluorinatedionomer and initiator to form the aqueous dispersion of particles offluorinated ionomer.
 2. The process of claim 1 wherein the amount ofsaid dispersion particulate of fluorinated ionomer provided in saidaqueous polymerization medium comprises less than about 15 wt % of saidfluorinated ionomer solids produced in said aqueous dispersion.
 3. Theprocess of claim 1 wherein said particulate of fluorinated ionomer havea weight average particle size of about 2 nm to about 100 nm.
 4. Theprocess of claim 1 wherein said fluorinated ionomer of said particulatehas an ion exchange ratio of about 3 to about
 53. 5. The process ofclaim 1 wherein said fluorinated ionomer of said particulate is highlyfluorinated.
 6. The process of claim 1 wherein said fluorinated ionomerof said particulate is perfluorinated.
 7. The process of claim 1 whereinsaid fluorinated ionomer of said particulate comprises a polymerbackbone with recurring side chains attached to the polymer backbonewith the side chains carrying ionic groups.
 8. The process of claim 1wherein said fluorinated ionomer of said particulate comprises ionicgroups having a pKa less than about
 10. 9. The process of claim 1wherein said fluorinated ionomer of said particulate comprises ionicgroups selected from the group consisting of sulfonate, carboxylate,phosphonate, phosphate and mixtures thereof.
 10. The process of claim 1wherein said fluorinated ionomer of said particulate comprises sulfonategroups.
 11. The process of claim 7 wherein said recurring side chainsare represented by the formula—(O—CF₂CFR_(f))_(a)—(O—CF₂)_(b)—(CFR′_(f))_(c)SO₃X, wherein R_(f) andR^(′) _(f) are independently selected from F, Cl or a perfluorinatedalkyl group having 1 to 10 carbon atoms, a=0 to 2, b=0 to 1, c=0 to 6,and X is H, Li, Na, K or NH₄.
 12. The process of claim 11 wherein saidrecurring side chain is represented by the formula—O—CF₂CF(CF₃)—O—CF₂CF₂—SO₃X wherein X is H, Li, Na, K or NH₄.
 13. Theprocess of claim 1 wherein said fluorinated ionomer of said particulatein thermoplastic form has a melt flow at 270° C. using a 5 kg weight ofabout 1 to about
 500. 14. The process of claim 1 further comprisingproviding surfactant in said polymerization medium.
 15. The process ofclaim 1 further comprising providing fluorosurfactant in saidpolymerization medium.
 16. The process of claim 1 further comprisingproviding fluoroether surfactant in said polymerization medium.
 17. Theprocess of claim 15 wherein said fluorosurfactant has the formula:[R¹-O_(n)-L-A⁻]Y⁺ wherein: R¹ is a linear or branched partially or fullyfluorinated aliphatic group which may contain ether linkages; n is 0 or1; L is a linear or branched alkylene group which may be nonfluorinated,partially fluorinated or fully fluorinated and which may contain etherlinkages; A⁻ is an anionic group selected from the group consisting ofcarboxylate, sulfonate, sulfonamide anion, and phosphonate; and Y⁺ ishydrogen, ammonium or alkali metal cation; with the proviso that thechain length of R¹-O_(n)-L- is not greater than 6 atoms.
 18. The processof claim 19 wherein n is
 1. 19. The process of claim 20 wherein R¹ isCF₃CF₂CF₂—; L is —CF(CF₃)—; and A⁻ is carboxylate; and Y⁺ is hydrogen orammonium.
 20. The process of claim 1 wherein said aqueous mediumcontains less than about 300 ppm of perfluoroalkane carboxylic acid orsalt fluorosurfactant having 8 or more carbon atoms based on the weightof water in said aqueous polymerization medium.
 21. The process of claim1 wherein said polymerizing produces less than about 13 wt % undispersedfluorinated ionomer based on the total weight of fluorinated ionomerproduced.
 22. The process of claim 1 wherein providing said dispersedfluorinated ionomer particulate in said aqueous polymerization medium isperformed by mixing concentrated aqueous liquid dispersion ordispersible powder of said fluorinated ionomer into said aqueouspolymerization medium.